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临床试验/NCT00300118
NCT00300118已完成3 期

Double-blind, Double-dummy, Randomized, Multicentre Study to Compare the Efficacy and Safety of Oral Budesonide (9 mg) and Oral Mesalazine (4.5 g) in Moderately Active Crohn's Disease Patients

Dr. Falk Pharma GmbH1 个研究点 分布在 1 个国家目标入组 311 人开始时间: 2004年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
311
试验地点
1
主要终点
Rate of remission

研究概览

简要总结

The purpose of this study is to determine whether mesalazine or budesonide is more active in the treatment of active Crohn's disease.

详细描述

Crohn's disease is often treated with glucocorticoids or mesalazine. Both drugs are indicated for active Crohn's disease. Treatment with mesalazine is indicated for the treatment of mildly to moderately active Crohn's disease. Budesonide 9 mg/day or mesalazine 4.5 g/day are better than lower doses.

So far only one trial compares the efficacy and safety of budesonide and 5-ASA. The result of this trial is that budesonide is more effective in inducing remission than mesalazine. The primary objective of this trial is to confirm this result for other presentations of budesonide and mesalazine; i.e. Budenofalk® capsules (9 mg/day) and Salofalk® tablets (Eudragit-L-coated oral mesalazine; 4.5 g/day) in moderately active Crohn's disease. Mesalazine is used in this trial as a comparator.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

A

Experimental

干预措施: budesonide (Drug)

B

Active Comparator

干预措施: mesalazine (Drug)

结局指标

主要结局

Rate of remission

次要结局

  • Response to treatment
  • Time to response
  • Time to remission
  • PGA
  • QoL

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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